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hereditary sensory neuropathy
(phenotype)
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Curated Studies
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Olfactory ecto-mesenchymal stem cells (OE-MSCs) from familial dysautonomia patients
Mouse Phenotypes - Hereditary peripheral neuropathy
OMIM - Neuropathy
OMIM - Pain
Fibroblasts with mutant ELP1 from familial dysautonomia patients treated with small molecule kinetin
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Literature
Most Relevant Literature
Cardiac arrest after anesthetic management in a patient with hereditary sensory autonomic neuropathy…
Hereditary sensory ataxic neuropathy associated with proximal muscle weakness in the lower extremiti…
A novel homozygous mutation in the WNK1/HSN2 gene causing hereditary sensory neuropathy type 2.
Hereditary sensory autonomic neuropathy caused by a mutation in dystonin.
DNMT1 links aberrant DNA methylation to hereditary sensory neuropathy.
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Clinical Trials
Most Relevant Clinical Trials
L-Serine Supplementation in Hereditary Sensory Neuropathy Type 1
Proprioception and Sensorimotor Control in Hereditary Sensory and Autonomic Neuropathy
Disability Severity Scale (DSI) and Hereditary Motor and Sensory Neuropathy Overall Disability Scale…
Topiramate for Cryptogenic Sensory Peripheral Neuropathy in Metabolic Syndrome (CSPN)
Early and Systematic Screening in Chronic Neuropathy
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